FDA applicant
K&J Consulting Corp.
FDA records 6 decisions for K&J Consulting Corp. (Lansdale, PA) from 2021 to 2025: 6 510(k) clearances. Most are in product codes ODP (Intervertebral Fusion Device With Bone Graft…) and KWQ (Appliance, Fixation, Spinal Intervertebral Body). Since 2016 its 510(k)s took a median of 60 days from receipt to decision, against 80 for FDA’s reviews in the same codes and years. Its devices cite 15 predicates, 2 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “K&J Consulting Corporation”, “K&J Consulting”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided K&J Consulting Corp.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2021.
Planning a device like K&J Consulting Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report